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FDA 510(k)

NEW VITAJET

K-Number: K851029 · 1985-05-23

ApplicantAndrew V. Stadler
Decision Date1985-05-23
Product CodeKZE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEW VITAJET is the device name listed in this FDA 510(k) record. The listed applicant is Andrew V. Stadler. It received FDA 510(k) clearance on 1985-05-23 under 510(k) number K851029. The device is classified under product code KZE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEW VITAJET?

NEW VITAJET is a medical device that received FDA 510(k) clearance on 1985-05-23. The listed applicant is Andrew V. Stadler. The 510(k) number is K851029.

When did NEW VITAJET receive FDA 510(k) clearance?

NEW VITAJET received FDA 510(k) clearance on 1985-05-23, under 510(k) number K851029.

Who is the listed applicant for NEW VITAJET?

The FDA 510(k) record lists Andrew V. Stadler as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEW VITAJET?

The FDA product code for NEW VITAJET is KZE.

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Related Devices (Code: KZE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K121270BIOJECT NEEDLE-FREE INJECTION MANAGEMENT SYSTEMBioject Medical Technologies, Inc.K111517PHARMAJET STRATIS 0.5 ML NEEDLE-FREE INJECTION SYSTEM MODEL 501-01, STRATIS INJECTOR CATALOG 501-10, STRATIS RESET STATIPharmajet, Inc.K110456PHARMAJET 0.1 ML INTRADERMAL NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.K090959LECTRAJET NEEDLE-FREE INJECTION SYSTEM, MODEL: M3 RAD'Antonio Consultants International, Inc. (Dci)K090003ZETAJETBioject, Inc.K081532PHARMAJET NEEDLE-FREE INJECTION SYSTEMPharmajet, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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